1435944-00-5

Upstream product

• 615-43-0 2-iodophenylamine 
• 598-32-3 2-hydroxy-3-butene 
• 61613-20-5 N-tosyl-2-iodoaniline 
• 1210801-46-9 N-(2-(bromomethyl)phenyl)-4-methyl-benzenesulfonamide 
• 90312-02-0 N-(2-hydroxymethylphenyl)-4-methylbenzenesulfonamide 
• 5344-90-1 2-Aminobenzyl alcohol 
• 98-59-9 p-toluenesulfonyl chloride 

Downstream Products

• 1202-04-6 indole-2-carboxylic acid methyl ester 
• 4264-35-1 2-acetylindole 
• 1627211-08-8 C₁₈H₂₁NO₂S 
• 1627210-65-4 C₁₉H₂₀N₂O₂S 
• 1627210-77-8 C₁₉H₂₀N₂O₂S 

Relevant academic research and scientific papers

Intramolecular aminocyanation of alkenes by N-CN bond cleavage

A metal-free, Lewis acid promoted intramolecular aminocyanation of alkenes was developed. B(C6F5)3 activates N-sulfonyl cyanamides, thus leading to a formal cleavage of the N-CN bonds in conjunction with vicinal addition o

Iodine-mediated intramolecular amination of ketones: The synthesis of 2-acylindoles and 2-acylindolines by tuning N-protecting groups

A general method for constructing both 2-acylindoles and 2-acylindolines via I2-mediated intramolecular C-N bond formation is presented, and the selective formation of either 2-acylindoles or 2-acylindolines just depends on the nitrogen protecting groups used in the same substrate skeletons. The Royal Society of Chemistry.